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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Phosphorothioic triamide, butyl-

CCCCNP(=S)(N)N Request for Quotation
Chemical Name: Phosphorothioic triamide, butyl-
CAS Number: 94317-64-3
Product Number: AG0036PH(AGN-PC-0JM06Q)
Synonyms:
MDL No:
Molecular Formula: C4H14N3PS
Molecular Weight: 167.2128

Identification/Properties

Properties
MP:
58-60°C
BP:
277.4°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
Stench
Computed Properties
Molecular Weight:
167.211g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
167.065g/mol
Monoisotopic Mass:
167.065g/mol
Topological Polar Surface Area:
96.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
110
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(n-Butyl)thiophosphoric triamide is a versatile reagent widely utilized in chemical synthesis for its unique properties and applications. Due to its strong nucleophilic nature, N-(n-Butyl)thiophosphoric triamide is commonly employed as a powerful reducing agent in various organic transformations. It is particularly useful in reactions requiring the reduction of various functional groups such as carbonyls, imines, and nitro compounds. The selective reactivity of this reagent allows for precise control over the reduction process, making it a valuable tool in the synthesis of complex organic molecules.Moreover, N-(n-Butyl)thiophosphoric triamide also finds application as a versatile coupling reagent in peptide synthesis. Its ability to facilitate amide bond formation between amino acids makes it an essential component in the preparation of peptides and other bioactive compounds. The high efficiency and selectivity of this reagent make it a preferred choice for chemists working in the field of medicinal chemistry and peptide synthesis.In addition to its role in reduction and coupling reactions, N-(n-Butyl)thiophosphoric triamide is utilized in various other processes such as deprotection of functional groups, ring-opening reactions, and cyclization reactions. Its compatibility with a wide range of functional groups and substrates makes it a valuable reagent for synthetic chemists seeking efficient and reliable methods for complex molecule synthesis.